The following data is part of a premarket notification filed by Pfm Produkte Fur Die Medizin Ag with the FDA for Multi-snare Set.
Device ID | K011783 |
510k Number | K011783 |
Device Name: | MULTI-SNARE SET |
Classification | Catheter, Embolectomy |
Applicant | PFM PRODUKTE FUR DIE MEDIZIN AG 15 CHEROKEE ST. Trabuco Canyon, CA 92679 |
Contact | Salvadore F Palomares |
Correspondent | Salvadore F Palomares PFM PRODUKTE FUR DIE MEDIZIN AG 15 CHEROKEE ST. Trabuco Canyon, CA 92679 |
Product Code | DXE |
CFR Regulation Number | 870.5150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-06-07 |
Decision Date | 2002-01-24 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
30813623011329 | K011783 | 000 |
04046964349317 | K011783 | 000 |
04046964349287 | K011783 | 000 |
00813623011564 | K011783 | 000 |
00813623011526 | K011783 | 000 |
00813623011519 | K011783 | 000 |
00813623011502 | K011783 | 000 |
00813623011557 | K011783 | 000 |
00813623011540 | K011783 | 000 |
04046964349331 | K011783 | 000 |
04046964349355 | K011783 | 000 |
04046964349379 | K011783 | 000 |
30813623011312 | K011783 | 000 |
30813623011305 | K011783 | 000 |
30813623011299 | K011783 | 000 |
30813623011282 | K011783 | 000 |
30813623011275 | K011783 | 000 |
30813623011268 | K011783 | 000 |
04046964349416 | K011783 | 000 |
04046964349393 | K011783 | 000 |
00813623011533 | K011783 | 000 |